过电位
纳米片
钯
催化作用
电催化剂
材料科学
硫黄
吸附
化学工程
溶解
无机化学
纳米技术
化学
电化学
物理化学
冶金
有机化学
电极
工程类
作者
Rui Zhu,Yizhen Wu,Jinyang Dai,Donghui Zhao,Zhicheng Wang,Hongyu Chen,Qiang Wang,Yawen Wang
出处
期刊:Small
[Wiley]
日期:2025-08-05
标识
DOI:10.1002/smll.202508542
摘要
Abstract With a S: Pd feeding ratio of 1: 100, Pd nanosheets (denoted as S 0.01 ‐Pd NSs) with wrinkled nanosheet morphology and polycrystalline structure that are almost indistinguishable with pristine Pd NSs are synthesized via a facile one‐pot solvothermal process. Notably, the trace amount of S‐incorporation (0.83 atom%) distinctively altered the surface electronic structure of the Pd NSs and boosted the performance of the S 0.01 ‐Pd NSs as oxygen reduction reaction (ORR) electrocatalyst. The S 0.01 ‐Pd NSs exhibited a half‐wave potential of 0.940 V, 12 mV more positive than that of the Pd NSs, and improved durability. Theoretical calculations with density functional theory indicated that the d ‐band center of the Pd(111) surface would shift increasingly negative with the amount of S incorporated. Furthermore, the adsorption, activation and hydrogenation of O 2 , would change drastically when the S‐incorporation increased from 3S to 4S on Pd(111) surface. The free energy changes in sequential ORR steps on the 3S‐Pd(111) surface are optimized, leading to a lower estimated overpotential compared to pristine Pd(111); while on 4S‐Pd(111) surface, ORR process is suppressed. Such a trend is consistent with the outstanding catalytical performance of the S 0.01 ‐Pd NSs, demonstrating that the trace‐amount incorporation is the optimized strategy for doping S in Pd‐based catalysts.
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